NCT06705179

Brief Summary

This study investigates the computational mechanisms associated with psychiatric disease dimensions. The study will characterize the relationship between computational parameter estimates of task performance and psychiatric symptoms and diagnoses with a longitudinal approach over a 12 month interval. Participants will be healthy participants recruited through Prolific an on-line crowdsourcing service, and psychiatric patients and healthy participants recruited via UCLA Psychiatry Clinics and UCLA's STAND Program

Trial Health

63
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Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
1,100

participants targeted

Target at P75+ for not_applicable

Timeline
45mo left

Started Jan 2025

Longer than P75 for not_applicable

Geographic Reach
1 country

2 active sites

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress27%
Jan 2025Dec 2029

First Submitted

Initial submission to the registry

November 18, 2024

Completed
8 days until next milestone

First Posted

Study publicly available on registry

November 26, 2024

Completed
1 month until next milestone

Study Start

First participant enrolled

January 1, 2025

Completed
5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

December 31, 2029

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2029

Last Updated

November 26, 2024

Status Verified

November 1, 2024

Enrollment Period

5 years

First QC Date

November 18, 2024

Last Update Submit

November 21, 2024

Conditions

Keywords

Computational PsychiatryBehavioral task battery

Outcome Measures

Primary Outcomes (6)

  • Changes in DASS depression scale scores

    Changes in computational parameter estimates related to gain/loss learning, reward/effort tradeoff and reward/predation risk tradeoffs will correlate with changes in DASS depression scale scores across time.

    12 months

  • Changes in DASS anxiety scale scores

    Changes in computational parameter estimates related to novelty driven exploration and reward/predation risk tradeoffs will be correlated with changes in DASS anxiety scale scores

    12 months

  • Changes in OCI-R scores

    Changes in computational parameter estimates related to the balance between model-based vs model-free reinforcement-learning will be correlated with changes in OCI-R symptoms across time.

    12 months

  • OCI-R scores

    Computational parameter estimates related to the balance between model-based vs model-free reinforcement-learning will be correlated with OCI-R scores.

    12 months

  • DASS depression scale scores

    Computational parameter estimates related to gain/loss learning, reward/effort tradeoff and reward/predation risk tradeoffs will correlate with DASS depression scale scores.

    12 months

  • DASS anxiety scale scores

    Computational parameter estimates related to novelty driven exploration and reward/predation risk tradeoffs will be correlated with DASS anxiety scale scores

    12 months

Study Arms (1)

Behavioral task battery

OTHER
Behavioral: Behavioral task performance

Interventions

Measures of performance on behavioral tasks

Behavioral task battery

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Age range of 18 to 65.
  • Not currently having a psychiatric diagnosis determined after psychiatric evaluation by Drs. Tadayon-Nejad and Wei (both are board certified psychiatrists).
  • Ability to understand and perform experimental tasks, i.e. basic ability to communicate and comprehend tasks.
  • Ability to give informed consent.

You may not qualify if:

  • Prior history and or current diagnosis of neurological disease.
  • Age range of 18 to 65.
  • Psychiatric diagnosis of any type of depressive disorders, any type of anxiety disorders or obsessive-compulsive disorder.
  • Primary or comorbid bipolar disorders are allowed but only if not in the acute manic phase.
  • Comorbidity with autism spectrum disorder (ASD) and attention-deficit/hyperactivity disorder (ADHD) are allowed.
  • Ability to understand and perform experimental tasks, i.e. basic ability to communicate and comprehend tasks.
  • Ability to give informed consent.
  • Prior history and or current diagnosis of neurological disease.
  • History or current diagnosis of psychotic disorders.
  • Currently active substance use disorder.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (2)

UCLA Semel Institute for Neuroscience and Human Behavior, University of California, Los Angeles

Los Angeles, California, 90095, United States

Location

California Insitute of Technology

Pasadena, California, 91125, United States

Location

MeSH Terms

Conditions

BehaviorDepressive DisorderAnxiety DisordersObsessive-Compulsive Disorder

Condition Hierarchy (Ancestors)

Mood DisordersMental Disorders

Study Officials

  • John P O'Doherty, D.Phil

    California Institute of Technology

    PRINCIPAL INVESTIGATOR

Central Study Contacts

John P O'Doherty, D.Phil

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Fletcher Jones Professor of Decision Neuroscience

Study Record Dates

First Submitted

November 18, 2024

First Posted

November 26, 2024

Study Start

January 1, 2025

Primary Completion (Estimated)

December 31, 2029

Study Completion (Estimated)

December 31, 2029

Last Updated

November 26, 2024

Record last verified: 2024-11

Data Sharing

IPD Sharing
Will share

Individual task performance data will be provided (trial data) and individual questionnaire scores will be available.

Shared Documents
ANALYTIC CODE
Access Criteria
Data will be provided to the NIH NDA database as requested per the grant conditions,

Locations